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Article

High-Mobility Group Box 1 Disrupts Metabolic Function with Cigarette Smoke Exposure in a Ceramide-Dependent Manner

1
Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84602, USA
2
College of Dental Medicine, Roseman University of Health Sciences, South Jordan, UT 84095, USA
3
Touchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390; USA
*
Author to whom correspondence should be addressed.
Academic Editor: Johannes Haybaeck
Int. J. Mol. Sci. 2017, 18(5), 1099; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051099
Received: 17 April 2017 / Revised: 16 May 2017 / Accepted: 18 May 2017 / Published: 20 May 2017
(This article belongs to the Special Issue Inhaled Pollutants Modulate Respiratory and Systemic Diseases)
We have previously found that cigarette smoke disrupts metabolic function, in part, by increasing muscle ceramide accrual. To further our understanding of this, we sought to determine the role of the cytokine high-mobility group box 1 (HMGB1), which is increased with smoke exposure, in smoke-induced muscle metabolic perturbations. To test this theory, we determined HMGB1 from lungs of human smokers, as well as from lung cells from mice exposed to cigarette smoke. We also treated cells and mice directly with HMGB1, in the presence or absence of myriocin, an inhibitor of serine palmitoyltransferase, the rate-limiting enzyme in ceramide biosynthesis. Outcomes included assessments of insulin resistance and muscle mitochondrial function. HMGB1 was significantly increased in both human lungs and rodent alveolar macrophages. Further testing revealed that HMGB1 treatment elicited a widespread increase in ceramide species and reduction in myotube mitochondrial respiration, an increase in reactive oxygen species, and reduced insulin-stimulated Akt phosphorylation. Inhibition of ceramide biosynthesis with myriocin was protective. In mice, by comparing treatments of HMGB1 injections with or without myriocin, we found that HMGB1 injections resulted in increased muscle ceramides, especially C16 and C24, which were necessary for reduced muscle mitochondrial respiration and compromised insulin and glucose tolerance. In conclusion, HMGB1 may be a necessary intermediate in the ceramide-dependent metabolic consequences of cigarette smoke exposure. View Full-Text
Keywords: high-mobility group box 1 (HMGB1); ceramides; mitochondrial bioenergetics; cigarette smoke high-mobility group box 1 (HMGB1); ceramides; mitochondrial bioenergetics; cigarette smoke
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MDPI and ACS Style

Taylor, O.J.; Thatcher, M.O.; Carr, S.T.; Gibbs, J.L.; Trumbull, A.M.; Harrison, M.E.; Winden, D.R.; Pearson, M.J.; Tippetts, T.S.; Holland, W.L.; Reynolds, P.R.; Bikman, B.T. High-Mobility Group Box 1 Disrupts Metabolic Function with Cigarette Smoke Exposure in a Ceramide-Dependent Manner. Int. J. Mol. Sci. 2017, 18, 1099. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051099

AMA Style

Taylor OJ, Thatcher MO, Carr ST, Gibbs JL, Trumbull AM, Harrison ME, Winden DR, Pearson MJ, Tippetts TS, Holland WL, Reynolds PR, Bikman BT. High-Mobility Group Box 1 Disrupts Metabolic Function with Cigarette Smoke Exposure in a Ceramide-Dependent Manner. International Journal of Molecular Sciences. 2017; 18(5):1099. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051099

Chicago/Turabian Style

Taylor, Oliver J., Mikayla O. Thatcher, Sheryl T. Carr, Jonathan L. Gibbs, Annie M. Trumbull, Mitchell E. Harrison, Duane R. Winden, Mackenzie J. Pearson, Trevor S. Tippetts, William L. Holland, Paul R. Reynolds, and Benjamin T. Bikman 2017. "High-Mobility Group Box 1 Disrupts Metabolic Function with Cigarette Smoke Exposure in a Ceramide-Dependent Manner" International Journal of Molecular Sciences 18, no. 5: 1099. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051099

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